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Medi

FDA UDI

Class II (US FDA UDI)

by Medi Manufacturing, Inc.

Identity

Trade Name
MEDI FDA UDI
Generic Name
Compression/pressure sock/stocking, single-use FDA UDI
Device Name
!SP20-30 COMF EW CLF PET NW BTB CT CHO V FDA UDI
Model / Reference
43X95 FDA UDI
Description
!SP20-30 COMF EW CLF PET NW BTB CT CHO V FDA UDI

Identifiers

Primary DI / UDI-DI
00636257185797 FDA UDI
FDA Product Code
DWL FDA UDI
GMDN Term
Compression/pressure sock/stocking, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Compression/pressure sock/stocking, single-use

A garment in the form of a sock or stocking, designed to provide graduated compression and pressure support for individuals with circulatory disorders. This device is intended for home use and clinical settings, and is intended to be used as a single-use solution.

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 47e498e9-b9a5-4f92-81c0-27bd763153b7 34 fields · synced Jul 21, 2026